Multiple open channel states revealed by lidocaine and QX-314 on rat brain voltage-dependent sodium channels

Abstract

We have recently reported that brain sodium channels display periods with high (low-K(d)) and low (high-K(d)) levels of lidocaine-induced open channel block (Salazar, B.C., D.O. Flash, J.L. Walewski, and E. Recio-Pinto, 1995. Brain Res. 699:305-314). In the present study, we further characterize this phenomenon by studying the effects of the permanently charged lidocaine analogue, QX-314. We found that the detection of high- and low-K(d) periods does not require the presence of the uncharged form of lidocaine. The level of block, for either period, at various QX-314 concentrations indicated the presence of a single local anesthetic binding site. Increasing the concentration of QX-314 decreased the lifetime of the high-K(d) periods while it increased the lifetime of the low-K(d) periods. These results could be best fitted to a model with two open channel conformations that display different local anesthetic K(d) values (low and high K(d)), and in which the channel area defining the local anesthetic K(d) consists of multiple interacting regions. Amplitude distribution analysis showed that changes in the K(d) values reflected changes in the k(on) rates, without changes in the k(off) rates. Both lidocaine and QX-314 were found to be incapable of blocking small-channel subconductance states (5-6 pS). Changes in the local anesthetic k(on) rates for blocking the fully open state and the lack of local anesthetic block of the small subconductance state are consistent with the presence of channel conformational changes involving the intracellular permeation pathway leading to the local anesthetic binding site.